Cao L - Search Results

1

Novel mutations in the SPAST gene cause hereditary spastic paraplegia.

Zhu Z, Zhang C, Zhao G, Liu Q, Zhong P, Zhang M, Tang W, Zhan F, Tian W, Wang Y, Yin K, Huang X, Jiang J, Liu X, Liu S, Zhou H, Luan X, Tang H, Wang Y, Chen S, Cao L. Zhu Z, et al. Among authors: cao l. Parkinsonism Relat Disord. 2019 Dec;69:125-133. doi: 10.1016/j.parkreldis.2019.11.007. Epub 2019 Nov 6. Parkinsonism Relat Disord. 2019. PMID: 31751864

2

[Mutation analysis of DJ1 gene in patients with autosomal recessive early-onset Parkinsonism].

Guo JF, Tang BS, Zhang YH, Xia K, Cai F, Pan Q, Shen L, Jiang H, Zhao GH, Yan XX, Cao L. Guo JF, et al. Among authors: cao l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Dec;22(6):641-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16331561 Chinese.

3

GIGYF2 Asn56Ser mutation is rare in Chinese Parkinson's disease patients.

Zhang Y, Zheng L, Zhang T, Wang Y, Xiao Q, Fei QZ, Cui PJ, Cao L, Chen SD. Zhang Y, et al. Among authors: cao l. Neurosci Lett. 2009 Oct 9;463(3):172-5. doi: 10.1016/j.neulet.2009.07.067. Epub 2009 Jul 26. Neurosci Lett. 2009. PMID: 19638301

4

CALHM1 P86L polymorphism is a risk factor for Alzheimer's disease in the Chinese population.

Cui PJ, Zheng L, Cao L, Wang Y, Deng YL, Wang G, Xu W, Tang HD, Ma JF, Zhang T, Ding JQ, Cheng Q, Chen SD. Cui PJ, et al. Among authors: cao l. J Alzheimers Dis. 2010;19(1):31-5. doi: 10.3233/JAD-2010-1207. J Alzheimers Dis. 2010. PMID: 20061624

5

Lack of association between ATP13A2 Ala746Thr variant and Parkinson's disease in Han population of mainland China.

Fei QZ, Cao L, Xiao Q, Zhang T, Zheng L, Wang XJ, Wang G, Zhou HY, Wang Y, Chen SD. Fei QZ, et al. Among authors: cao l. Neurosci Lett. 2010 May 14;475(2):61-3. doi: 10.1016/j.neulet.2010.03.018. Epub 2010 Mar 19. Neurosci Lett. 2010. PMID: 20227461

6

Four novel mutations in the GCH1 gene of Chinese patients with dopa-responsive dystonia.

Cao L, Zheng L, Tang WG, Xiao Q, Zhang T, Tang HD, He SB, Wang XJ, Ding JQ, Chen SD. Cao L, et al. Mov Disord. 2010 Apr 30;25(6):755-60. doi: 10.1002/mds.22646. Mov Disord. 2010. PMID: 20437540

7

Transthyretin-related hereditary amyloidosis in a Chinese family with TTR Y114C mutation.

Zhang Y, Deng YL, Ma JF, Zheng L, Hong Z, Wang ZQ, Sheng CY, Xiao Q, Cao L, Chen SD. Zhang Y, et al. Among authors: cao l. Neurodegener Dis. 2011;8(4):187-93. doi: 10.1159/000321679. Epub 2010 Dec 3. Neurodegener Dis. 2011. PMID: 21135536

8

Novel mutations in the CYP7B1 gene cause hereditary spastic paraplegia.

Cao L, Fei QZ, Tang WG, Liu JR, Zheng L, Xiao Q, He SB, Fu Y, Chen SD. Cao L, et al. Mov Disord. 2011 Jun;26(7):1354-6. doi: 10.1002/mds.23466. Epub 2011 Mar 30. Mov Disord. 2011. PMID: 21452256 No abstract available.

9

Genetic polymorphisms in sigma-1 receptor and apolipoprotein E interact to influence the severity of Alzheimer's disease.

Huang Y, Zheng L, Halliday G, Dobson-Stone C, Wang Y, Tang HD, Cao L, Deng YL, Wang G, Zhang YM, Wang JH, Hallupp M, Kwok J, Chen SD. Huang Y, et al. Among authors: cao l. Curr Alzheimer Res. 2011 Nov;8(7):765-70. doi: 10.2174/156720511797633232. Curr Alzheimer Res. 2011. PMID: 21605063

10

DJ-1 modulates the expression of Cu/Zn-superoxide dismutase-1 through the Erk1/2-Elk1 pathway in neuroprotection.

Wang Z, Liu J, Chen S, Wang Y, Cao L, Zhang Y, Kang W, Li H, Gui Y, Chen S, Ding J. Wang Z, et al. Among authors: cao l. Ann Neurol. 2011 Oct;70(4):591-9. doi: 10.1002/ana.22514. Epub 2011 Jul 27. Ann Neurol. 2011. PMID: 21796667

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